Skeletal Muscle Ultrasound: Correlation Between Fibrous Tissue and Echo Intensity

2009 ◽  
Vol 35 (3) ◽  
pp. 443-446 ◽  
Author(s):  
Sigrid Pillen ◽  
Ramon O. Tak ◽  
Machiel J. Zwarts ◽  
Martin M.Y. Lammens ◽  
Kiek N. Verrijp ◽  
...  
2021 ◽  
Vol 102 (10) ◽  
pp. e26
Author(s):  
Matthew Rong Jie Tay ◽  
Jong Moon Kim ◽  
Deshan Kumar Rajeswaran ◽  
Shuen-Loong Tham ◽  
Wen Li Lui ◽  
...  

2010 ◽  
Vol 43 (1) ◽  
pp. 142-143 ◽  
Author(s):  
Jacqueline Nijboer-Oosterveld ◽  
Nens Van Alfen ◽  
Sigrid Pillen

2018 ◽  
Vol Volume 13 ◽  
pp. 1871-1878 ◽  
Author(s):  
Yuya Watanabe ◽  
Masahiro Ikenaga ◽  
Eiichi Yoshimura ◽  
Yosuke Yamada ◽  
Misaka Kimura

2020 ◽  
Author(s):  
Julien Anais ◽  
Kanagalingam Anuya ◽  
Megret Jérome ◽  
Luka Marine ◽  
Ménager Mickaël ◽  
...  

AbstractTissue regeneration relies on the activation of tissue resident stem cells concomitant with a transient fibrous tissue deposition to allow functional tissue recovery. Bone regeneration involves skeletal stem/progenitors from periosteum and bone marrow, the formation of a fibrous callus followed by the deposition of cartilage and bone to consolidate the fracture. Here, we show that mesenchymal progenitors residing in skeletal muscle adjacent to the bone fracture play a crucial role in mediating the initial fibrotic response to bone injury and also participate in cartilage and bone formation in the fracture callus. Combined lineage and scRNAseq analyses reveal that skeletal muscle mesenchymal progenitors adopt a fibrogenic fate before they engage in a chondrogenic fate after fracture. In polytrauma, where bone and skeletal muscle are injured, skeletal muscle mesenchymal progenitors fail to undergo fibrogenesis and chondrogenesis. This leads to impaired healing and persistent callus fibrosis originating from skeletal muscle. Thus, essential bone-muscle interactions govern bone regeneration through the direct contribution of skeletal muscle as a source of mesenchymal progenitors driving the fibrotic response and fibrotic remodeling, and supporting cartilage and bone formation.


Author(s):  
Amanda Vale-Lira ◽  
Natália Turri-Silva ◽  
Kenneth Verboven ◽  
João Luiz Quagliotti Durigan ◽  
Alexandra Corrêa de Lima ◽  
...  

Exercise intolerance, a hallmark of patients with heart failure (HF), is associated with muscle weakness. However, its causative microcirculatory and muscle characteristics among those with preserved or reduced ejection fraction (HFpEF or HFrEF) phenotype is unclear. The musculoskeletal abnormalities that could result in impaired peripheral microcirculation are sarcopenia and muscle strength reduction in HF, implying lowered oxidative capacity and perfusion affect transport and oxygen utilization during exercise, an essential task from the microvascular muscle function. Besides that, skeletal muscle microcirculatory abnormalities have also been associated with exercise intolerance in HF patients who also present skeletal muscle myopathy. This cross-sectional study aimed to compare the muscle microcirculation dynamics via near-infrared spectroscopy (NIRS) response during an isokinetic muscle strength test and ultrasound-derived parameters (echo intensity was rectus femoris muscle, while the muscle thickness parameter was measured on rectus femoris and quadriceps femoris) in heart failure patients with HFpEF and HFrEF phenotypes and different functional severities (Weber Class A, B, and C). Twenty-eight aged-matched patients with HFpEF (n = 16) and HFrEF (n = 12) were assessed. We found phenotype differences among those with Weber C severity, with HFrEF patients reaching lower oxyhemoglobin (O2Hb, μM) (−10.9 ± 3.8 vs. −23.7 ± 5.7, p = 0.029) during exercise, while HFpEF reached lower O2Hb during the recovery period (−3.0 ± 3.4 vs. 5.9 ± 2.8, p = 0.007). HFpEF with Weber Class C also presented a higher echo intensity than HFrEF patients (29.7 ± 8.4 vs. 15.1 ± 6.8, p = 0.017) among the ultrasound-derived variables. Our preliminary study revealed more pronounced impairments in local microcirculatory dynamics in HFpEF vs. HFrEF patients during a muscle strength exercise, combined with muscle-skeletal abnormalities detected via ultrasound imaging, which may help explain the commonly observed exercise intolerance in HFpEF patients.


2007 ◽  
Vol 17 (7) ◽  
pp. 509-516 ◽  
Author(s):  
S. Pillen ◽  
A. Verrips ◽  
N. van Alfen ◽  
I.M.P. Arts ◽  
L.T.L. Sie ◽  
...  

2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 716.2-716
Author(s):  
A. Tripoli ◽  
S. Barsotti ◽  
A. Delle Sedie ◽  
G. Aringhieri ◽  
S. Vitali ◽  
...  

Background:Muscle involvement is the most frequent clinical feature in patients with idiopathic inflammatory myopathies (IIM). In addition to muscular enzymes, muscular magnetic resonance has been investigated for the assessment of disease activity, but it is limited by high costs and it is not readily available. Muscle ultrasound (MUS) has been recently proposed as a valuable tool for the diagnosis and activity assessment of muscle involvement in IIM patients.Objectives:To define the role of MUS in the diagnosis and assessment of disease activity in IIM through quantitative analysis of MUSMethods:This was a prospective study conducted from February 2019 to November 2019. 41 patients with IIM: 17 men and 24 women, median age 61.4 years, of which 20 were polymyositis (PM), 16 dermatomyositis (DM) and 5 inclusion body myositis (IBM) were included. 30 healthy subjects (HS), comparable in age and gender to patients, were recruited as controls. In every patient and control MUS of upper and lower extremities was performed (in total 10 muscles per side) and digital images were saved. Quantitative muscle echo intensity (QME) was calculated using an image processing program (ImageJ) to obtain the mean value of greyscale (mGS) for each muscle. For patients with IIM creatine phosphokinase (CPK) levels were recorded, duration of disease (in months) was calculated and clinical evaluation tools for the assessment of disease activity were performed, such as manual muscle testing (MMT8), patient and physician visual analogue scales (pVAS, phVAS), health assessment questionnaire (HAQ) and myositis disease activity assessment tool (MDAAT).Results:Patients had higher values of mGS across all muscles examined than controls (p<0.001). Among patients QME showed a negative correlation with MMT8 (p<0.001, -0.641<r<-0.412), but no correlation with CPK levels or duration of disease. A positive correlation was found between QME and HAQ (p<0.05; 0.320<r<0.599), pVAS (0.003<p<0.046; 0.314<r<0.455) and phVAS (0.029<p<0.002; 0.341<r<0.471). No significant correlation was found between QME and MDAAT and no statistically significant differences of muscle echo intensity were observed between patients with IBM, DM and PM.Conclusion:Quantitative analysis of MUS showed to be useful to differentiate IIM patients from healthy subjects, therefore it could be a helpful technique to screen patients with muscular symptoms in which perform additional investigations. In our study, the data collected did not allow to assess the disease activity of IIM patients and did not allow to distinguish between the 3 different subgroups of IIM patients, but further studies may help in the identification of different muscular patterns to guide the clinical suspect and the possible role of MUS in the follow-up of the patients.Disclosure of Interests:Alessandra Tripoli: None declared, Simone Barsotti: None declared, Andrea Delle Sedie Speakers bureau: MSD, Lilly, Novartis, Abbvie, Celgene, Giacomo Aringhieri: None declared, Saverio Vitali: None declared, Rossella Neri: None declared, Davide Caramella: None declared, Marta Mosca: None declared


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